Signs & Symptoms
Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.
Amyotrophic lateral sclerosis
Very frequent (80-99%)HP:0007354
Parkinsonian disease
Frequent (30-79%)HP:0001300
Progressive dementia
Frequent (30-79%)HP:0000726
Abnormal sexual behavior
HP:0008768
Archaic reflex
HP:0002476
Diminished volitional state
HP:0000745
Frontal lobe dementia
HP:0000727
Frontotemporal dementia
HP:0002145
Impulse control disorders
HP:0000734
Inappropriate laughter
HP:0000748
Increased appetite
HP:0002591
Irritable mood
HP:0000737
Lack of feeling, emotion, interest
HP:0000741
Language impairment
HP:0002463
Mouthing
HP:0000710
Neuronal loss in CNS
HP:0002529
Personality changes
HP:0000751
Related Conditions
Frontal lobe degeneration with motor neurone disease(child)
Frontotemporal dementia with gene located on 3p11(child)
Right temporal atrophy variant frontotemporal dementia(child)
Behavioral variant of frontotemporal dementia(child)
Pick's disease with Pick bodies(child)
Pick's disease with Pick cells and no Pick bodies(child)
Semantic dementia(child)
Dementia due to Pick's disease(child)
Amyotrophic lateral sclerosis with frontotemporal dementia(child)
Dementia due to neurofilament inclusion body disease(child)
Frontotemporal dementia due to TARDBP mutation(child)
Frontotemporal dementia due to valosin containing protein mutation(child)
Frontotemporal dementia due to chromosome 9 open reading frame 72 mutation(child)
Frontotemporal dementia due to FUS mutation(child)
Hereditary dysphasic disinhibition dementia(child)
Lobar atrophy(parent)
Dementia(parent)
Quick Facts
- SNOMED CT
- 230270009
- UMLS CUI
- C0338451
- Fully Specified Name
- Frontotemporal dementia (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 17
Medical Disclaimer
This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.
Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.